LGR5型
癌症干细胞
干细胞
脂质体
阿霉素
Wnt信号通路
癌症研究
药物输送
癌细胞
癌症
生物
转移
药理学
化学
细胞生物学
化疗
生物化学
信号转导
有机化学
遗传学
作者
Jing Cao,Chong Li,Xiaohui Wei,Meiqing Tu,Yan Zhang,Fengwei Xu,Yuhong Xu
出处
期刊:Molecular Cancer Therapeutics
[American Association for Cancer Research]
日期:2018-07-01
卷期号:17 (7): 1475-1485
被引量:15
标识
DOI:10.1158/1535-7163.mct-17-0694
摘要
Abstract Cancer stem cells (CSC) that may account for only a small fraction of tumor mass were found to play crucial roles during tumor initiating, progression, and metastasis. However, they are usually difficult to be treated and notoriously resilient to drug eradication. In this study, we aimed at the Wnt signaling characteristic of CSCs and designed a liposomal drug delivery system to target CSCs. Liposomes decorated with RSPO1 on the surface were constructed for specific interactions with the Wnt pathway coreceptor LGR5. Doxorubicin carried by the RSPO1-liposomes was more effective at lower concentrations than the same drug loaded in PEG-liposomes. More importantly, we showed using a patient-derived xenograft tumor model where LGR5+ CSCs coexisted with LGR5− cells, the RSPO1-liposomes were able to access more CSC cells and deliver the drug specifically and efficiently. Such a focused effect in eradicating LGR5+ cells led to massive tumor tissue necrosis and growth inhibition even when only a fraction of the conventional drug dose was used. These data clearly demonstrated the advantages of CSC-targeted drug delivery and would support the development of such approaches as a new cancer treatment strategy. Mol Cancer Ther; 17(7); 1475–85. ©2018 AACR.
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